Mackenzie's Chance - Update 3/6/2010
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Uploaded by alabambelle on Mar 6, 2010
Mackenzie's Chance - Update on my granddaughter Mackenzie LeClair Jackson who has been suffering from a rare kidney desease since she was born on November 17, 2008. We have been back here in Birmingham, AL since February 1st because Mackenzie suffered a collapsed lung and had to be flown back to UAB Children's Hospital. After staying in the hospital for 2 1/2 weeks we are now living at the Ronald McDonald house in Birmingham because Mackenzie has to have Hemo Dialysis 4 days a week and it is too far to drive back and forth from our hometown. But on March 11th Mackenzie will receive a very "Special Gift"...A New Kidney! Some very Special Person wanted to donate one of their kidneys to a small child and Mackenzie was the "Perfect Match". We are so Thankful to this person for giving our little Angel a second chance. We hope to meet this person so we can let them know how Thankful we are. We just can't Thank them enough. God Bless them always for being so giving. I hope you enjoy my little update on Mackenzie, if so please comment and rate. I don't know if I will get a chance to reply because we are so busy with Mackenzie, but I do want you to know that I really appreciate all the comments that are left here. Please continue to pray for Mackenzie, her Wonderful Donor and her loving family. Prayers do help and they mean alot to us. Thank You All So Very Much!When you have the time please check out Children's Health Care Systems of AL YT Website, this is where Mackenzie has spent most of her life. It is a wonderful hospital, the videos there will prove it. The YT site is: CHSYSORG. Take care and God Bless! HUGS! Your friend, Sandra
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Uploader Comments (alabambelle)
All Comments (53)
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Sandra she is so gorgeous!!! I can't believe she's over a year old already. Time flies by doesn't it!!! I'm keeping everything crossed for you (which makes me look very silly when I try to walk :-) ) Loe to you all!! You're always in my thoughts xx
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God bless you baby girl ,me and lil Hadyn is praying for you. so glad you got your gift of life . baby girl we know what you and your family has been going through we are so glad it's for the most part over take care of each other be bless. maybe 1 day all the CNS babies can have a play day after all our transplants are done. what a wonderful gift you are so beautiful sending love from Hadyn allyssa our transplant is april 15th hope to see you soon.
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Praying all has gone well~What a princess she is!!
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wonderful videos - no words to say what I 'm feeling!! 5*****
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This indeed is an amazing story!!!
This splendid video brought tears to my eyes!!!
I will definitely be keeping you all in my prayers!!!
Lots of love & Best Wishes to you all ♥
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Great video of a precious child. You will have a new day to celebrate every year now.... March 11.
Don
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Thankyou Sandra for making this beautiful video of little Mackenzie our thoughts and prayers are with you
Love your utube friend Carol
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@mariehes749, Part 2, He is a little fighter just like Mackenzie and all the other children who fight this desease, and when he gets a new kidney you will see a big difference in him. It is a difficult time to go through but so worth it. God will get him thru this so keep your faith going. I am putting your family along with John on my prayer list. Please stay in touch on my channel and let me know how he is. Take Care and God Bless! Sandra
alabambelle 3 months ago
Hi your grand daughter is just amazing. I wanted to say thank you so much my son John has been born wih the same as Mackenzie he is now 4 and a half months oldcurrently on albumin 3 times a week we come home in between. Your story gives us alot of faith and hope that John will see this through. So thank you for taking the time a very grateful mum Mariexxx P.S Much Love and best wishes to you and your family xxx
mariehes749 3 months ago in playlist More videos from alabambelle
@mariehes749, Hi Marie, Thank You So much for stopping by my channel to view this video and for the wonderful comment you left. Mackenzie was also born with this desease and spent a big part of her life in the hospital on Albumin and then Dialysis. Since her kidney transplant she has done very well and is at home being like a normal little girl should be. I know what you are going thru but your precious little boy will get thru this. Part 2 will continue.
alabambelle 3 months ago